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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261229Generated: November 3, 2026

Acetamide → 4-(4-Bromophenyl)-2-methyl-1,3-oxazole

https://huagongshe.com/reaction/2261229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamideHCID 178—
Reactant4-Bromophenacyl bromideHCID 7454—
Product4-(4-Bromophenyl)-2-methyl-1,3-oxazoleHCID 1287310722.5%

Reaction Steps

4-Bromophenacyl bromide (21.3 g) and acetamide (11.3 g) were heated together at 130° C. under argon. After 2.5 h the reaction mixture was allowed to cool, and partitioned between water (150 ml) and Et2O (150 ml). The organic phase was washed with aqueous NaOH (0.5N), aqueous HCl (0.5M) and saturated aqueous NaCl solution (100 ml) of each), dried (MgSO4) and evaporated to give a brown solid which was recrystallised from hexanes to give the title compound (D14) as an orange solid (4.1 g). LCMS electrospray (+ve) 239 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846922B2
Source datasetuspto-grants-2010_12
ORD IDord-39e0a8e3431d438d9ecd53f964349d49
Source noteuspto-grants-2010_12